Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6809854
LOC105376976
1.000 0.040 3 18742931 intron variant A/G snv 0.19 1
rs7007032
CSMD1
1.000 0.040 8 3821924 intron variant C/T snv 0.75 1
rs7071642
ZNF365 ; LOC105378327
1.000 0.040 10 62654300 intron variant G/A snv 0.81 1
rs887466
POU5F1 ; PSORS1C3
1.000 0.040 6 31175734 intron variant G/A snv 0.40 1
rs9304742
ZNF816-ZNF321P
1.000 0.040 19 52948038 intron variant T/C snv 0.42 1
rs9504361
EXOC2
1.000 0.040 6 577820 intron variant A/G snv 0.40 1
rs953861
LOC285626
1.000 0.040 5 159345574 intron variant G/A;C snv 1
rs963986
CAVIN1
1.000 0.040 17 42409561 intron variant G/C snv 0.15 1
rs13437088 0.925 0.040 6 31387342 intergenic variant C/T snv 0.32 5
rs1062470
PSORS1C1 ; CDSN
0.925 0.040 6 31116658 synonymous variant G/A snv 0.37 0.41 4
rs657555
PTPN2
0.925 0.080 18 12847137 intron variant C/A;T snv 3
rs10852936
ZPBP2
0.925 0.120 17 39875461 intron variant C/T snv 0.39 0.40 2
rs1250546
ZMIZ1
0.925 0.080 10 79272775 intron variant A/G snv 0.36 2
rs2082412 0.925 0.120 5 159290781 downstream gene variant G/A snv 0.27 2
rs492602
LOC105447645 ; FUT2
0.925 0.120 19 48703160 synonymous variant A/G snv 0.38 0.45 2
rs495337
SPATA2
0.925 0.120 20 49905793 synonymous variant G/A snv 0.44 0.35 2
rs1056198
RNF114
0.925 0.040 20 49939692 intron variant C/T snv 0.34 1
rs11593576
ZMIZ1
0.925 0.040 10 79256139 intron variant C/T snv 0.29 1
rs12445568
STX1B
0.925 0.040 16 30993491 splice region variant T/C snv 0.39 0.38 1
rs1265181
PSORS1C3
0.925 0.040 6 31188008 intergenic variant G/C snv 0.15 1
rs17716942
KCNH7
0.925 0.040 2 162404181 intron variant T/C snv 9.6E-02 1
rs2066807
STAT2
0.925 0.080 12 56346898 missense variant C/G snv 4.9E-02 4.6E-02 1
rs2066819
STAT2
0.925 0.040 12 56356420 intron variant C/T snv 4.9E-02 4.5E-02 1
rs2233278
TNIP1
0.925 0.040 5 151087628 5 prime UTR variant G/C;T snv 4.8E-02 1
rs27432
ERAP1 ; LOC102724748
0.925 0.040 5 96783569 intron variant A/C;G snv 1